CR10879A - CYCLIZED DERIVATIVES AS EG-5 INHIBITORS - Google Patents
CYCLIZED DERIVATIVES AS EG-5 INHIBITORSInfo
- Publication number
- CR10879A CR10879A CR10879A CR10879A CR10879A CR 10879 A CR10879 A CR 10879A CR 10879 A CR10879 A CR 10879A CR 10879 A CR10879 A CR 10879A CR 10879 A CR10879 A CR 10879A
- Authority
- CR
- Costa Rica
- Prior art keywords
- inhibitors
- cyclized derivatives
- cyclized
- derivatives
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88374007P | 2007-01-05 | 2007-01-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CR10879A true CR10879A (en) | 2009-08-05 |
Family
ID=39577804
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CR10879A CR10879A (en) | 2007-01-05 | 2009-06-19 | CYCLIZED DERIVATIVES AS EG-5 INHIBITORS |
Country Status (30)
| Country | Link |
|---|---|
| US (3) | US7820646B2 (en) |
| EP (1) | EP2106399A2 (en) |
| JP (1) | JP2010515687A (en) |
| KR (1) | KR20090097210A (en) |
| CN (1) | CN101622247A (en) |
| AR (1) | AR064760A1 (en) |
| AU (1) | AU2008205169B2 (en) |
| BR (1) | BRPI0806264A2 (en) |
| CA (1) | CA2674318A1 (en) |
| CL (1) | CL2008000029A1 (en) |
| CO (1) | CO6561828A2 (en) |
| CR (1) | CR10879A (en) |
| DO (1) | DOP2009000169A (en) |
| EA (1) | EA200900924A1 (en) |
| EC (1) | ECSP099485A (en) |
| GE (1) | GEP20125415B (en) |
| GT (1) | GT200900192A (en) |
| HN (1) | HN2009001262A (en) |
| MA (1) | MA31080B1 (en) |
| MX (1) | MX2009007260A (en) |
| NI (1) | NI200900134A (en) |
| NZ (1) | NZ577727A (en) |
| PE (1) | PE20081850A1 (en) |
| SM (1) | SMP200900065B (en) |
| SV (1) | SV2009003325A (en) |
| TN (1) | TN2009000287A1 (en) |
| TW (1) | TW200836722A (en) |
| UA (1) | UA97821C2 (en) |
| WO (1) | WO2008086122A2 (en) |
| ZA (1) | ZA200904175B (en) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8252832B2 (en) | 2007-12-14 | 2012-08-28 | Novartis Ag | Kinesin inhibitors as cancer therapeutics |
| EA201201404A1 (en) | 2010-04-15 | 2013-04-30 | Новартис Аг | TRIAZOLE AS KVB INHIBITORS (KINESIN-PROTEIN VERETEN) |
| WO2011128388A2 (en) * | 2010-04-15 | 2011-10-20 | Novartis Ag | Oxazole and thiazole compounds as ksp inhibitors |
| EP2390247A1 (en) | 2010-05-26 | 2011-11-30 | Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability) | Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde |
| GB201113538D0 (en) | 2011-08-04 | 2011-09-21 | Karobio Ab | Novel estrogen receptor ligands |
| EP2968591A1 (en) * | 2013-03-15 | 2016-01-20 | Novartis AG | Cell proliferation inhibitors and conjugates thereof |
| US9498540B2 (en) | 2013-03-15 | 2016-11-22 | Novartis Ag | Cell proliferation inhibitors and conjugates thereof |
| CN106163568B (en) * | 2013-12-23 | 2021-03-23 | 拜耳制药股份公司 | Antibody Drug Conjugates (ADC) containing spindle Kinesin (KSP) |
| EP3310440A1 (en) * | 2015-06-22 | 2018-04-25 | Bayer Pharma Aktiengesellschaft | Antibody drug conjugates (adcs) and antibody prodrug conjugates (apdcs) with enzymatically cleavable groups |
| CN105367506B (en) * | 2015-12-08 | 2021-02-05 | 华润双鹤药业股份有限公司 | Preparation method of chiral high piperazine ring |
| CN105330657B (en) * | 2015-12-08 | 2019-05-21 | 华润双鹤药业股份有限公司 | The preparation method of the chloro- 2- of 5- [5- (R)-methyl-1,4- Diazesuberane -1-] benzoxazoles |
| JP7022707B2 (en) | 2016-06-15 | 2022-02-18 | バイエル・ファルマ・アクティエンゲゼルシャフト | Specific antibody-drug-conjugate (ADC) including KSP inhibitor and anti-CD123 antibody |
| PE20191235A1 (en) | 2016-12-21 | 2019-09-11 | Bayer Pharma AG | LIGAND-DRUG CONJUGATES (ADCS) WITH ENZYMATICALLY CLEARABLE GROUPS |
| EP3558387B1 (en) | 2016-12-21 | 2021-10-20 | Bayer Pharma Aktiengesellschaft | Specific antibody drug conjugates (adcs) having ksp inhibitors |
| CA3103327A1 (en) | 2018-06-18 | 2019-12-26 | Bayer Aktiengesellschaft | Binder/active agent conjugates directed against cxcr5, having enzymatically cleavable linkers and improved activity profile |
| CN119859151A (en) * | 2023-10-19 | 2025-04-22 | 北京振东光明药物研究院有限公司 | Alkaloid compound separated from rhizoma smilacis glabrae and preparation method and application thereof |
Family Cites Families (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2550959C3 (en) | 1975-11-13 | 1980-12-04 | Hoechst Ag, 6000 Frankfurt | Tetrazolyl-imidazoles and tetrazolyl-benzimidazoles, processes for their preparation and pharmaceuticals containing them |
| US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| US4501728A (en) | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
| GB2157285B (en) | 1984-04-11 | 1987-10-28 | Erba Farmitalia | 1h, 7h-pyrazolo1, 5-a pyrimidine-7-one derivatives and process for their preparation |
| US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| US4837028A (en) | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| US5859012A (en) * | 1996-04-03 | 1999-01-12 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| JP2001505585A (en) | 1996-12-16 | 2001-04-24 | 藤沢薬品工業株式会社 | Novel amide compounds and their use as nitric oxide synthase inhibitors |
| US6117940A (en) | 1997-10-17 | 2000-09-12 | Mjalli; Adnan M. M. | Amino-ketone solid support templates |
| US6172087B1 (en) | 1998-06-03 | 2001-01-09 | Gpi Nil Holding, Inc. | N-oxide of heterocyclic ester, amide, thioester, or ketone hair growth compositions and uses |
| US6271241B1 (en) | 1999-04-02 | 2001-08-07 | Neurogen Corporation | Cycloalkyl and aryl fused aminoalkyl-imidazole derivatives: modulators and GLP-1 receptors |
| EP1165519A1 (en) | 1999-04-02 | 2002-01-02 | Neurogen Corporation | Aryl and heteroaryl fused aminoalkyl-imidazole derivatives and their use as antidiabetics |
| TWI292316B (en) | 1999-10-11 | 2008-01-11 | Sod Conseils Rech Applic | Pharmaceutical composition of thiazole derivatives intended to inhibit mao and/or lipidic peroxidation and/or to act as modulators of sodium channels and the use thereof |
| US7291641B2 (en) | 1999-10-11 | 2007-11-06 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Derivatives of heterocycles with 5 members, their preparation and their use as medicaments |
| US20040132788A1 (en) | 1999-10-11 | 2004-07-08 | Chabrier De Lassauniere Pierre-Etienne | Derivatives of heterocycles with 5 members, their preparation and their use as medicaments |
| US6545004B1 (en) | 1999-10-27 | 2003-04-08 | Cytokinetics, Inc. | Methods and compositions utilizing quinazolinones |
| BR0015110A (en) | 1999-10-27 | 2002-07-02 | Cytokinetics Inc | Methods of treating cell proliferative diseases, of treating a disorder associated with ksp kinesin activity, of ksp kinesin inhibition, of kps kinesin modulators and of screening compounds that bind ksp kinesin, and compounds |
| WO2001083575A1 (en) | 2000-05-02 | 2001-11-08 | Advanced Syntech, Llc A Kentucky Limited Liability Corporation | A novel solid support template for preparation of highly functionalized heterocycle compounds |
| WO2001094318A2 (en) | 2000-06-05 | 2001-12-13 | Ortho-Mcneil Pharmaceutical, Inc. | Method for synthesis of substituted azole libraries |
| US6683191B2 (en) | 2000-06-05 | 2004-01-27 | Ortho-Mcneil Pharmaceuticals, Inc. | Method for synthesis of substituted azole libraries |
| ES2282275T3 (en) | 2000-08-01 | 2007-10-16 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | IMIDAZOLIL DERIVATIVES |
| MXPA03003039A (en) | 2000-10-06 | 2003-10-15 | Neurogen Corp | Benzimidazole and indole derivatives as crf receptor modulators. |
| AU2002221239A1 (en) | 2000-12-07 | 2002-06-18 | Astrazeneca Ab | Therapeutic benzimidazole compounds |
| US6964967B2 (en) | 2000-12-11 | 2005-11-15 | Amgen, Inc. | Substituted pyrido[2,3-d]pyrimidines and methods for their use |
| WO2002057244A1 (en) | 2001-01-19 | 2002-07-25 | Cytokinetics, Inc. | Phenothiazine kinesin inhibitors |
| US20040132830A1 (en) | 2001-01-19 | 2004-07-08 | Finer Jeffrey T | Triphenylmethane kinesin inhibitors |
| EP1444209A4 (en) | 2001-11-07 | 2005-02-16 | Merck & Co Inc | INHIBITORS OF MITOTIC KINESIN |
| US6753428B2 (en) | 2001-11-20 | 2004-06-22 | Cytokinetics, Inc. | Process for the racemization of chiral quinazolinones |
| WO2003049527A2 (en) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| ATE372341T1 (en) | 2001-12-06 | 2007-09-15 | Merck & Co Inc | INHIBITORS OF MITOTIC KINESIN |
| JP4467979B2 (en) | 2001-12-06 | 2010-05-26 | メルク・シャープ・エンド・ドーム・コーポレイション | Mitotic kinesin inhibitor |
| JP2005515208A (en) | 2001-12-06 | 2005-05-26 | メルク エンド カムパニー インコーポレーテッド | Mitotic kinesin inhibitor |
| JP4391825B2 (en) | 2001-12-06 | 2009-12-24 | メルク エンド カムパニー インコーポレーテッド | Mitotic kinesin inhibitor |
| WO2003059289A2 (en) | 2002-01-10 | 2003-07-24 | Neurogen Corporation | Melanin concentrating hormone receptor ligands: substituted benzoimidazole analogues |
| WO2003070701A2 (en) | 2002-02-15 | 2003-08-28 | Cytokinetics, Inc. | Syntheses of quinazolinones |
| WO2003079973A2 (en) | 2002-03-08 | 2003-10-02 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| US7026312B2 (en) | 2002-03-14 | 2006-04-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Substituted piperidines, pharmaceutical compositions containing these compounds, their use and processes for the preparation thereof |
| DE10211770A1 (en) | 2002-03-14 | 2003-10-02 | Boehringer Ingelheim Pharma | Novel substituted piperidines, pharmaceutical compositions containing them and processes for their preparation |
| ATE471931T1 (en) | 2002-04-17 | 2010-07-15 | Cytokinetics Inc | COMPOUNDS, COMPOSITIONS AND METHODS |
| GB0209995D0 (en) | 2002-05-01 | 2002-06-12 | Merck Sharp & Dohme | Therapeutic agents |
| US7030144B2 (en) | 2002-05-02 | 2006-04-18 | Neurogen Corporation | Substituted imidazole derivatives: GABAA receptor ligands |
| US6982268B2 (en) | 2002-05-08 | 2006-01-03 | Neurogen Corporation | Substituted imidazolylmethyl pyridine and pyrazine derivatives GABAA receptor ligands |
| AU2003270015A1 (en) | 2002-05-09 | 2003-12-02 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| WO2003094839A2 (en) | 2002-05-09 | 2003-11-20 | Cytokinetics, Inc. | Pyrimidinone compounds, compositions and methods |
| WO2004026226A2 (en) | 2002-05-10 | 2004-04-01 | Cytokinetics, Inc. | Compounds, compositions and methods |
| AU2003237881A1 (en) | 2002-05-17 | 2003-12-02 | Neurogen Corporation | Substituted ring-fused imidazole derivates: gabaa receptor ligands |
| JP2005536475A (en) | 2002-05-23 | 2005-12-02 | サイトキネティクス・インコーポレーテッド | Compounds, compositions and methods |
| US20050234080A1 (en) * | 2002-05-23 | 2005-10-20 | Coleman Paul J | Mitotic kinesin inhibitors |
| US7301028B2 (en) | 2002-06-14 | 2007-11-27 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| EP1556357A4 (en) | 2002-06-14 | 2006-09-13 | Cytokinetics Inc | Compounds, compositions, and methods |
| KR20050010515A (en) | 2002-06-14 | 2005-01-27 | 머크 앤드 캄파니 인코포레이티드 | Mitotic kinesin inhibitors |
| WO2004004652A2 (en) | 2002-07-08 | 2004-01-15 | Merck & Co., Inc. | Mitotic kinesin binding site |
| WO2004006865A2 (en) | 2002-07-17 | 2004-01-22 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| EP1537089A4 (en) | 2002-07-23 | 2008-04-16 | Cytokinetics Inc | Compounds compositions and methods |
| AU2003262747A1 (en) | 2002-08-21 | 2004-03-11 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| JP2005539062A (en) | 2002-09-13 | 2005-12-22 | サイトキネティクス・インコーポレーテッド | Compounds, compositions and methods |
| CN100579579C (en) | 2002-10-01 | 2010-01-13 | 诺华疫苗和诊断公司 | Anti-cancer and anti-infectious disease compositions and methods of use thereof |
| ATE335732T1 (en) | 2002-11-08 | 2006-09-15 | Neurogen Corp | 4-IMIDAZOLE-1-YLMETHYLPYRIMIDENE DERIVATIVES AS LIGANDS FOR GABAA RECEPTORS |
| EP1581520A4 (en) * | 2002-12-13 | 2006-08-23 | Smithkline Beecham Corp | Compounds, compositions and methods |
| WO2004064741A2 (en) | 2003-01-17 | 2004-08-05 | Cytokinetics Inc. | Compounds, compositions, and methods |
| WO2004071448A2 (en) | 2003-02-12 | 2004-08-26 | Transtech Pharma Inc. | Substituted azole derivatives as inhibitors of protein tyrosine phosphatases |
| US20080021079A1 (en) | 2003-05-07 | 2008-01-24 | Han-Jie Zhou | Compounds, Compositions, and Methods |
| JP2007500746A (en) | 2003-05-15 | 2007-01-18 | サイトキネティクス・インコーポレーテッド | Compounds, compositions and methods |
| WO2004113335A2 (en) | 2003-06-20 | 2004-12-29 | Chiron Corporation | Pyridino[1,2-a]pyrimidin-4-one compounds as anticancer agents |
| WO2005041888A2 (en) * | 2003-11-03 | 2005-05-12 | Cytokinetics, Inc. | Pyrimidin-4-one compounds, compositions and methods |
| NZ548208A (en) | 2004-02-12 | 2010-09-30 | Transtech Pharma Inc | Substituted azole derivatives, compositions, and methods of use |
| PT1732926E (en) | 2004-04-06 | 2009-04-03 | Novartis Vaccines & Diagnostic | Mitotic kinesin inhibitors |
| EP1740550A1 (en) | 2004-04-14 | 2007-01-10 | Pfizer Limited | Sulphur-linked imidazole compounds for the treament of hiv |
| US7618981B2 (en) | 2004-05-06 | 2009-11-17 | Cytokinetics, Inc. | Imidazopyridinyl-benzamide anti-cancer agents |
| CA2564215A1 (en) | 2004-05-21 | 2005-12-01 | Chiron Corporation | Substituted quinoline derivatives as mitotic kinesin inhibitors |
| JP4836280B2 (en) * | 2004-06-18 | 2011-12-14 | ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド | N- (1- (1-benzyl-4-phenyl-1H-imidazol-2-yl) -2,2-dimethylpropyl) benzamide derivatives and related as kinesin spindle protein (KSP) inhibitors for the treatment of cancer Compound |
| KR20070072598A (en) | 2004-10-19 | 2007-07-04 | 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 | Indole and benzimidazole derivatives |
| TW200800951A (en) | 2005-08-09 | 2008-01-01 | Novartis Ag | Substituted imidazole compounds as KSP inhibitors |
| MX2009005071A (en) | 2006-11-13 | 2009-05-25 | Novartis Ag | Substituted pyrazole and triazole compounds as ksp inhibitors. |
-
2008
- 2008-01-03 CA CA002674318A patent/CA2674318A1/en not_active Abandoned
- 2008-01-03 KR KR1020097016289A patent/KR20090097210A/en not_active Withdrawn
- 2008-01-03 GE GEAP200811346A patent/GEP20125415B/en unknown
- 2008-01-03 EP EP08705667A patent/EP2106399A2/en not_active Withdrawn
- 2008-01-03 JP JP2009544977A patent/JP2010515687A/en active Pending
- 2008-01-03 NZ NZ577727A patent/NZ577727A/en not_active IP Right Cessation
- 2008-01-03 CN CN200880007148A patent/CN101622247A/en active Pending
- 2008-01-03 AU AU2008205169A patent/AU2008205169B2/en not_active Ceased
- 2008-01-03 WO PCT/US2008/050149 patent/WO2008086122A2/en not_active Ceased
- 2008-01-03 MX MX2009007260A patent/MX2009007260A/en not_active Application Discontinuation
- 2008-01-03 US US11/969,164 patent/US7820646B2/en not_active Expired - Fee Related
- 2008-01-03 EA EA200900924A patent/EA200900924A1/en unknown
- 2008-01-03 BR BRPI0806264-1A patent/BRPI0806264A2/en not_active IP Right Cessation
- 2008-01-04 CL CL200800029A patent/CL2008000029A1/en unknown
- 2008-01-04 TW TW097100432A patent/TW200836722A/en unknown
- 2008-01-04 AR ARP080100042A patent/AR064760A1/en not_active Application Discontinuation
- 2008-01-04 PE PE2008000091A patent/PE20081850A1/en not_active Application Discontinuation
- 2008-03-01 UA UAA200906929A patent/UA97821C2/en unknown
-
2009
- 2009-06-15 ZA ZA200904175A patent/ZA200904175B/en unknown
- 2009-06-19 CR CR10879A patent/CR10879A/en unknown
- 2009-06-30 MA MA32061A patent/MA31080B1/en unknown
- 2009-07-02 DO DO2009000169A patent/DOP2009000169A/en unknown
- 2009-07-02 CO CO09068496A patent/CO6561828A2/en not_active Application Discontinuation
- 2009-07-02 NI NI200900134A patent/NI200900134A/en unknown
- 2009-07-03 GT GT200900192A patent/GT200900192A/en unknown
- 2009-07-03 HN HN2009001262A patent/HN2009001262A/en unknown
- 2009-07-03 TN TNP2009000287A patent/TN2009000287A1/en unknown
- 2009-07-03 EC EC2009009485A patent/ECSP099485A/en unknown
- 2009-07-03 SV SV2009003325A patent/SV2009003325A/en not_active Application Discontinuation
- 2009-07-23 SM SM200900065T patent/SMP200900065B/en unknown
-
2010
- 2010-09-15 US US12/882,473 patent/US20110003791A1/en not_active Abandoned
-
2012
- 2012-04-03 US US13/438,569 patent/US20120189623A1/en not_active Abandoned
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